Laura Pérez‐Cano
Impact in
- Molecular Medicine top 5%
- Antibiotic Resistance in Bacteria
- Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Bacterial Genetics and Biotechnology
Papers in
-
- RNA and protein synthesis mechanisms 7
- RNA Research and Splicing 7
- RNA modifications and cancer 6
- Genetics 9
- Genetics and Neurodevelopmental Disorders 7
- Co-authors
- Juan Fernández‐Recio (13 shared papers)Carles Pons (4 shared papers)Albert Solernou (4 shared papers)Solène Grosdidier (3 shared papers)Lee-kai Wang (3 shared papers)Daniel H. Geschwind (3 shared papers)Jennifer K. Lowe (3 shared papers)Michael J. Gandal (2 shared papers)
- Journals
- Proteins Structure Function and Bioinformatics (5 papers)Biomedicines (2 papers)Nucleic Acids Research (2 papers)Proceedings of the National Academy of Sciences (2 papers)Human Genetics and Genomics Advances (1 paper)
- Partner nations
- SpainUnited StatesCanada
In The Last Decade
Laura Pérez‐Cano
23 papers receiving 941 citations
Hit Papers
Peers
Comparison fields: 5 of 88
- Molecular Medicine 91
- Genetics 304
- Cognitive Neuroscience 189
- Molecular Biology 629
- Biochemistry 62
Countries citing papers authored by Laura Pérez‐Cano
This map shows the geographic impact of Laura Pérez‐Cano's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Laura Pérez‐Cano with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laura Pérez‐Cano more than expected).
Fields of papers citing papers by Laura Pérez‐Cano
This network shows the impact of papers produced by Laura Pérez‐Cano. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Laura Pérez‐Cano. The network helps show where Laura Pérez‐Cano may publish in the future.
Co-authors
The 25 scholars most cited alongside Laura Pérez‐Cano, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks Hit paper breakdown → | 2019 | 257 |
| 2 | 2008 | 138 | |
| 3 | 2009 | 80 | |
| 4 | 2014 | 73 | |
| 5 | 2009 | 72 | |
| 6 | 2009 | 53 | |
| 7 | 2023 | 44 | |
| 8 | 2012 | 43 | |
| 9 | 2021 | 39 | |
| 10 | 2015 | 37 | |
| 11 | 2010 | 23 | |
| 12 | 2010 | 21 | |
| 13 | 2013 | 19 | |
| 14 | 2016 | 15 | |
| 15 | 2021 | 11 | |
| 16 | 2013 | 9 | |
| 17 | 2023 | 7 | |
| 18 | 2010 | 4 | |
| 19 | 2024 | 2 | |
| 20 | 2019 | 2 |
About Laura Pérez‐Cano
Laura Pérez‐Cano is a scholar working on Molecular Biology, Genetics, Cognitive Neuroscience, Computational Theory and Mathematics and Psychiatry and Mental health, having authored 23 papers that have together received 952 indexed citations. Recurring topics across this work include RNA and protein synthesis mechanisms (7 papers), Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (7 papers), RNA Research and Splicing (7 papers), RNA modifications and cancer (6 papers), Attention Deficit Hyperactivity Disorder (3 papers), Computational Drug Discovery Methods (3 papers) and Enzyme Structure and Function (3 papers). The work is most often cited by research in Molecular Medicine (91 citations), Genetics (304 citations), Cognitive Neuroscience (189 citations), Molecular Biology (629 citations) and Biochemistry (62 citations). Laura Pérez‐Cano has collaborated with scholars based in Spain, United States and Canada. Frequent co-authors include Juan Fernández‐Recio, Carles Pons, Albert Solernou, Solène Grosdidier, Lee-kai Wang, Daniel H. Geschwind, Jennifer K. Lowe, Michael J. Gandal, Dennis P. Wall and Jae-Yoon Jung. Their work appears in journals such as Proteins Structure Function and Bioinformatics, Biomedicines, Nucleic Acids Research, Proceedings of the National Academy of Sciences and Human Genetics and Genomics Advances.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.